A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498382



Internal ID22556317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177434181..177441292hg38UCSC Ensembl
chr5:176861182..176868293hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387112
hg197112
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841620
Supporting Variants
Samples
Known GenesGRK6, PRR7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498382
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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